FDA OKs Q-Collar Device to Protect Athletes’ Brains During Head Impacts

The U.S. Food and Drug Administration (FDA) authorized marketing of a new device to be worn around the neck of athletes aged 13 years and older during sports to protect the brain from effects associated with repetitive sub-concussive head impacts. Q30 Sports Science’s Q-Collar non-invasive C-shaped collar applies compressive force to the neck and increases blood volume to help reduce brain movement within the cranial space, which may occur during head impacts. The device may reduce occurrence of specific changes in the brain associated with brain injury.
 
“Today’s action provides an additional piece of protective equipment athletes can wear when playing sports to help protect their brains from the effects of repetitive head impacts while still wearing the personal protective equipment associated with the sport,” Christopher M. Loftus, M.D., acting director of the Office of Neurological and Physical Medicine Devices in the FDA’s Center for Devices and Radiological Health told the press.
 
Traumatic brain injury (TBI) can be caused by a forceful bump, blow, or jolt to the head or body, or from an object that pierces the skull and enters the brain. Not all blows or jolts to the head result in a TBI. The National Institute of Neurological Disorders and Stroke notes anywhere from 1.6 million to 3.8 million sports- and recreation-related TBIs are estimated to occur in the U.S. annually.
 
When worn around the neck during sports, the Q-Collar provides compressive force to the internal jugular veins, increasing blood volume in the skull’s blood vessels. Typically, when people experience blunt trauma accidents, the brain moves unrestrained in the skull, which is known as a “slosh.” The Q-Collar’s increase in blood volume in those vessels creates a tighter fit of the brain inside the skull and reduces “slosh” movement. By reducing the movement of the brain within the cranial space, the Q-Collar may aid in the protection of the brain from the effects of head impacts.
 
The FDA assessed the safety and effectiveness of the Q-Collar through several studies, including a prospective, longitudinal study in the United States with 284 subjects 13 years or older who were participants on a high school football team. During the sports season, 139 athletes wore the Q-Collar and 145 athletes did not. All participants also wore an accelerometer device that measured every impact to the head sustained during play. Each athlete underwent a magnetic resonance imaging (MRI) scan pre-season and post-season. These MRI scans were used to generate Diffusion Tensor Imaging (a specialized MRI image) of the brain that allowed researchers to compare structural changes in the participants’ brain, after a season of play.
 
Significant changes were found in deeper tissues of the brain involved in the transmission of electrical nerve signals (white matter regions) in 106 of the 145 (73 percent) participants in the no-Collar group, while no significant changes in these regions were found in 107 of the 139 (77 percent) of the group who wore the Q Collar. These differences appear to indicate protection of the brain associated with device use. No significant adverse events were associated with device use.
 
The Q-Collar does not replace, and should be worn with, other protective sports equipment associated with specific sports activities, such as helmets and shoulder pads. Wearers of the device should not depend on the device to protect them from all harmful effects of head impacts. Users should take steps to avoid direct impact to the head and neck. Data do not demonstrate that the device can prevent concussion or serious head injury. The Q-Collar should not be used if an individual has not been medically cleared to play contact sports.
 
The Q-Collar has not been tested and should not be used on athletes with the following conditions:
 

• Increased pressure in the skull (including uncontrolled ocular-glaucoma)
• Increased presence of acid in the body or excessive blood alkalinity
• Open head injury (including in or around the eye) within the past six months
• Pseudotumor cerebri (false brain tumor)
• Presence of brain or spinal shunt
• Accumulation of cerebrospinal fluid within the brain
• Known seizure disorder
• Known trachea abnormality
• Known airway obstruction
• Known carotid hypersensitivity
• Blood clot in the brain
• Increased likelihood of blood clotting (coagulation)
• Collections of small blood vessels in the brain that are enlarged and irregular in structure
• Skin injury, rash, or other abnormality on or around the neck

 
The device can be worn for up to four hours at a time and should be replaced after two years of active use or upon the product’s expiration date listed on the package, whichever comes first. The Q-Collar is intended for over-the-counter use and will be distributed directly to consumers. However, a medical professional should be consulted if a user is unsure whether the Q-Collar is right for him or her.
 
The FDA reviewed the device through the De Novo premarket review pathway.